Wire and pulley clock mechanism flow regulator

ABSTRACT

An automatic injection device with flow regulation. The automatic injection device has an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also has a fluid path which fluidly connects the drug container to the patient via an insertion needle, a potential energy source, and a regulator configured to restrict release of potential energy and restrict linear movement of the plunger and the pharmaceutical product into the fluid path at a proscribed pace. The regulator includes a clock escapement mechanism and a wire and pulley system including a wire coupled to at least one pulley. The potential energy source may be a spring that surrounds the drug container and may be directly coupled to the plunger and the wire such that movement of the spring and the wire is restricted over time.

PRIORITY CLAIM

This application claims priority under 35 U.S.C. § 119 to U.S. Provisional Application No. 62/535,083, filed on Jul. 20, 2017 which is expressly incorporated by reference herein in its entirety.

SUMMARY

The present disclosure is directed to flow regulation of an automatic injection device utilizing a wire and pulley clock mechanism. The automatic injection device includes an insertion needle configured to be inserted into a patient and a drug container which contains a pharmaceutical product and includes a plunger. The automatic injection device also includes a fluid path which fluidly connects the drug container to the insertion needle, a potential energy source, and a regulator configured to cause a predefined, possibly linear movement of the plunger to force the pharmaceutical product into the fluid path at a proscribed pace. The potential energy source may be a spring contained inside the drug container and may be directly coupled to the back of the plunger. The clock escapement mechanism applies a counterforce and thus restricts movement of the spring and plunger in a controlled rate over a specified time interval, using a gearbox and a wire and pulley system directly attached to the spring.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a side view illustration of an exemplary automatic injection device positioned on a patient;

FIG. 2 is a schematic illustration of the components of an automatic injection device consistent with disclosed embodiments;

FIG. 3 is a perspective view of a top side of the automatic injection device;

FIG. 4 is a perspective view of a bottom side of the automatic injection device;

FIG. 5 is a perspective view of the internal components according to an embodiment of the automatic injection device;

FIG. 6 is a perspective view of the internal components of a clock, incorporated in an embodiment of the clock escapement mechanism for the regulator.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Injection devices are used to deliver pharmaceutical products such as biologics and medications to a patient (i.e., a person or animal). A syringe and needle is an example of a widely-used injection device. This basic system typically involves a person manually moving a plunger portion of the syringe to force the pharmaceutical product through the needle and into the patient. Other injection devices have been developed to deliver pharmaceutical products automatically at the touch of a button or the actuation of a switch. These devices are advantageous in that they allow a patient to more easily self-administer the pharmaceutical product. Moreover, some automatic injection devices allow for slow or periodic delivery of the pharmaceutical product as needed, which is a typical procedure for patients dependent on insulin injections, for example. However, there is a need for automatic injection devices to provide increased injection control in a compact device such that the device is easy to handle and discrete for a patient who may wear the device for an extended period of time.

Disclosed embodiments pertain to a regulator for an automatic injection device. For example, the regulator may be configured to control movement of a plunger placed in a drug container. Further movement of the plunger inside the drug container pushes the pharmaceutical product through a fluid path and to an insertion needle which connects to the patient. This controlled movement of the plunger allows for metered delivery of the pharmaceutical product according to desired parameters.

The disclosed regulator includes features which allow for precise control over plunger movement which is based on stored potential energy while providing a small form factor which allows the automatic injection device to be compact. The disclosed regulator utilizes a clock escapement mechanism and a potential energy source in order to control movement of the plunger. In the embodiment set forth in the drawings and as described hereinafter, the potential energy source is a spring that may directly push the connected plunger; but that is just by way of example. In other embodiments, any potential energy source may be utilized, including compressed air.

Current energy sources for automatic injection devices utilize springs as an energy source for pumping the pharmaceutical product out of the device and into a patient. These springs, however, apply a variable force because the force of the spring is relative to its displacement. This varies the velocity and rate of infusion.

In contrast, the described embodiments regulate potential energy in a proscribed regulated pace. In the embodiment set forth in the drawings and as described hereinafter, the disclosed regulator includes a mechanical clock escapement mechanism utilizing a wire and pulley system that restricts movement of the spring over a specified period of time for more restricted and controlled release. Thus, the clock escapement mechanism controls the plunger so that the velocity of the potential energy source and rate of infusion is constant. This configuration allows for a cost-effective, space saving alternative to control the movement of the plunger with a passive, mechanical driving device. This configuration, when totally mechanical, can undergo sterilization procedures that a unit with electronics may not be able to utilize.

It should be understood that other types of regulators may be used in place of a clock mechanism, and one of skill in the art may utilize other mechanical mechanisms in order to restrict and regulate the movement of the plunger. In some embodiments, the clock escapement mechanism may be connected to a device which further regulates the spring over a specified time interval. This restriction of movement of the spring may restrict movement of the plunger and thus movement of the pharmaceutical product out of the drug container over time (e.g., and into a patient through a fluid path).

FIG. 1 is a depiction of an exemplary embodiment of an automatic injection device 12 on a patient 10. The patient 10 is not limited and can be any organism which may receive an injection. The device 12 is configured to deliver a pharmaceutical product to the patient 10 automatically. This means that the device 12 is controlling the injection in some way such that the system differs from other injection systems where manual input alone causes the injection (i.e., a conventional syringe and needle system or other available systems). The automatic aspect of the device 12 may additionally or alternatively relate to the duration of the injection, controlled injection intervals, a delay between input and injection, etc.

The device 12 includes a base 14 that contacts the patient's skin. The device 12 includes an insertion needle 16 which enters a patient to deliver a pharmaceutical product, such as insulin, to the patient. An example of an automatic injection device which includes many of the features that may be incorporated into the device 12 is described in WO 2017/007952, which is herein incorporated by reference. However, it should be understood that the device 12 is not limited to the automatic injection device described therein or the exemplary embodiments described below. An automatic injection device consistent with this disclosure may include some of the features described herein but is not limited thereto. For example, a disclosed automatic injection device may resemble a syringe and needle system or other injection system, which is adapted for automatic injections via the features described herein.

FIG. 2 is a schematic illustration of the automatic injection device 12 and flow regulator 24 and the basic features of the device 12 which facilitate automatic injections of a pharmaceutical product into the patient 10. The device 12 preferably includes a housing 18 which holds at least some of the features of the device 12. In addition to the insertion needle 16, these features preferably include a drug container 20, a fluid path 22, a regulator 24 and potential energy source 26. These features work in conjunction with each other to automatically and mechanically deliver a pharmaceutical product to the patient 10 according to desired parameters.

The regulator 24 provides the automatic aspect of the injections via device 12. For example, the regulator 24 is a mechanical system which restricts movement of the pharmaceutical product from the drug container 20 to the fluid path 22 and ultimately into the patient 10 at a proscribed pace. In the embodiment described in the drawings and hereinafter, the regulator 24 mechanically regulates movement of a plunger (not depicted). In other embodiments, the regulator 24 may include both a mechanical unit and a small electrical unit that may exert a minimal amount of energy for regulating movement of the plunger and release of the fluid at a proscribed pace. For example, in one embodiment, the regulator 24 may include a ratchet mechanism that releases potential energy from the potential energy source at a certain pace and exerts a small fraction of energy in order to stop the mechanism in a required pace. The ratchet may be stopped and released by a small electrical unit such as a solenoid or a different actuator. In addition, in another embodiment, the regulator may control the flow between the needle and the fluid path by periodically obstructing fluid flow.

The drug container 20 is a containing element which supplies the pharmaceutical product. The drug container 20 may be a vial, syringe, or the like and includes a space for containing the pharmaceutical product, which is not limited to a particular substance. The pharmaceutical product may be any substance which is considered one or more of a drug, biologic, medication, or placebo, for example. The drug container 20 is preferably a hollow cylindrical tube which receives the pharmaceutical product. However, it should be understood that other configurations are possible.

In the device 12, the drug container 20 is fluidly connected to the insertion needle 16 by the fluid path 22. The fluid path 22 may be a physical connecting channel which serves as a conduit for delivering the pharmaceutical product from the drug container 20 to the insertion needle 16 and ultimately into the patient 10. The fluid path 22 may include additional structure, including actuating mechanisms which initiate delivery of the pharmaceutical product and/or control mechanisms which meter an amount of product which is delivered to the patient 10 at any particular time. The fluid path 22 may include an element or mechanism which is configured to establish the connecting channel, such as a puncturing needle or the like. The fluid path 22 may be associated with a mechanical start button or control switch which control an element of the fluid path 22 (e.g., a valve) in order to start or stop the delivery of the pharmaceutical product. It should be understood, however, that the fluid path 22 may be a passive system component in at least some embodiments.

FIGS. 3 and 4 further illustrate an exemplary embodiment of the automatic injection device 12. FIG. 3 illustrates a first side of the device 12, including the housing 18 which rests on top of the base 14. The housing 18 is illustrated as being rectangular, but can include any shape. The housing 18 may include optional features such as a window 30 which provides a view of the drug container 20 and thus the current fluid level.

FIG. 4 illustrates a second side of the device 12 including a bottom surface of the base 14. The bottom surface 32 includes an opening 34 for receiving the insertion needle 16. In use, the device 12 is placed against the patient 10 with the bottom surface 32 of the base 14 against the skin. An injection needle extends through the opening 34 and into the patient 10 to deliver the pharmaceutical product. The bottom surface 32 may include an adhesive material thereon to adhere the device 12 to the patient 10 for either a short or long period of time, depending on the particular use of the device 12.

FIG. 5 illustrates the device 12 incorporating the flow regulator 24 having a wire and pulley system with the top portion of the housing 18 removed such that the internal features are shown in an enclosed space 36 formed by a lower portion of the housing 18 and the base 14. The device 12 includes exemplary embodiments of the insertion needle 16, the drug container 20, the fluid path 22, and the regulator 24. The enclosed space 36 houses at least the drug container 20 and the regulator 24 such that the elements are positioned inside of the housing 18.

The fluid path 22 in this embodiment includes a connector 38 which physically connects to the drug container 20 to establish a connection channel between the interior of the drug container 20 and the insertion needle 16. In the illustrated embodiment, the insertion needle 16 is positioned perpendicular to the drug container 20 such that the path of the pharmaceutical product is to travel out of the drug container 20 and laterally into the area of the insertion needle 16 via the fluid path 22. The pharmaceutical product subsequently travels vertically downward through the insertion needle 16 and into the patient 10. This configuration is exemplary, however, and the disclosed embodiments are not limited thereto. In other embodiments, the insertion needle 16 may be aligned in the same direction as the drug container 20 and/or the fluid path 22.

In the present embodiment, the regulator 24 includes a clock escapement mechanism 40 and a pulley system 54 that includes a wire 54A. The clock escapement mechanism 40 includes a set of gears 40A coupled to the pulley system 54. In one embodiment, the clock escapement mechanism 40 inhibits movement of the spring 44 via the gears 40A and the wire 54A and the pulley system 54, by applying a counterforce to the spring 44. The wire 54A of the pulley system 54 may be coupled to a set of pulleys 54B and connected to the spring 44 itself. The movement of the wire 54A and the pulley system 54 controls and restricts movement of the spring 44 inside the drug container 20, which controls and restricts movement of the plunger 50 in a linear motion inside the drug container 20.

In the embodiments set forth in the drawings and described hereinafter, the spring 44 is positioned inside of the drug container 20 and is connected to the plunger 50 directly, but this is just by way of example. The direct connection between the spring 44 and the plunger 50 may move the spring 44 and thus the plunger 50 forward at a controlled proscribed pace during release of the pharmaceutical product. The spring 44 may be positioned behind the drug container 20 and connected to the plunger 50, such that the spring 44 pushes the plunger 50 during release of the pharmaceutical product.

FIG. 5 depicts the spring in a resting position, as fluid stored in the drug container 20 is completely released into the fluid path 22. The clock escapement mechanism 40 is configured to slowly allow the spring 44 to move between settings to the resting positions over a specified time interval via the wire 54A and the pulley system 54. The wire 54A and the pulley system 54 may be coupled to the spring at a first longitudinal end 46 of the drug container 20. As a result, movement of the wire 54A along the pulley 54B moves the spring 44.

When fluid is stored in the drug container 20, the spring 44 is wound and stored potentially energy increases until release of the fluid into the fluid path 22 during injection via the plunger 50. During injection, the clock escapement mechanism 40 restricts movement of the wire 54A and the pulley system 54. The wire 54A and the pulley system 54 thus restricts unwinding of the spring 44 at a controlled pace. In the process of unwinding and returning to a resting position, the spring 44 pushes the plunger 50 incrementally as controlled by the wire 54A of the pulley system 54, toward a second longitudinal end 48 of the drug container 20, thereby forcing the pharmaceutical product into the fluid path 22 and ultimately delivering it to the patient 10 through the insertion needle 16 in a controlled manner over the specified time interval, as needed. Other mechanisms may be utilized in order to control movement of the plunger 50 if the spring 44 is not directly connected to the plunger 50. It should be noted that in other embodiments, other mechanisms for connecting the spring 44 and the plunger 50 to control movement may also be utilized.

FIG. 6 is a perspective view of the internal components of a clock incorporated in an embodiment of the clock escapement mechanism 40 for the regulator 24. Components of the escapement mechanism of the clock may be similar to the clock escapement mechanism 78, which includes an escape wheel 78A and a pallet 78B. In the present embodiment, the clock escapement mechanism 78 further regulates the periodic movement of the gear 40A, 40C (not depicted), while, the balance wheel 74 is operatively coupled to the escapement mechanism 78 via the pallet 78B.

When the spring 44 begins to move, the escapement mechanism 78, the balance wheel 74, and the gear 40A begin to move. As the balance wheel 74 moves rotationally, clockwise and counterclockwise periodically, the movement releases a tooth of the escape wheel 78A of the escapement mechanism 78. The release of the tooth of the escape wheel 78A allows the gear 40A (not depicted) to only advance by a fixed amount. This regular periodic advancement moves the gear 40A in a controlled and restricted manner. This control also restricts movement of the wire 54A and the pulley system 54 (not depicted), which further restricts movement of the spring 44 (not depicted) over a time interval. This configuration enables delivery of the pharmaceutical product at a more controlled rate over a specified time.

Having thus described the presently preferred embodiments in detail, it is to be appreciated and will be apparent to those skilled in the art that many physical changes, only a few of which are exemplified in the detailed description of the invention, could be made without altering the inventive concepts and principles embodied therein. It is also to be appreciated that numerous embodiments incorporating only part of the preferred embodiment are possible which do not alter, with respect to those parts, the inventive concepts and principles embodied therein. The present embodiments and optional configurations are therefore to be considered in all respects as exemplary and/or illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all alternate embodiments and changes to this embodiment which come within the meaning and range of equivalency of said claims are therefore to be embraced therein. 

What is claimed is:
 1. An automatic injection device, comprising: a drug container which contains a pharmaceutical product, the drug container including a plunger and a potential energy source configured to release potential energy; a fluid path which connects the drug container to an insertion needle; and a regulator comprising: a clock escapement mechanism comprising at least one set of gears, and a wire directly coupled to at least one pulley, the at least one set of gears, and the potential energy source, the wire directly coupled to the potential energy source at a first longitudinal end of the drug container; wherein the potential energy source pushes the plunger toward a second longitudinal end of the drug container, and wherein the regulator applies a counterforce to the potential energy source to restrict release of the potential energy from the potential energy source over a proscribed period of time.
 2. The automatic injection device of claim 1, wherein the at least one set of gears comprises: a pallet and an escape wheel gear configured to restrict a regular periodic movement of the potential energy source by a fixed amount that restricts release of the potential energy over a time interval.
 3. The automatic injection device of claim 2, wherein the clock escapement mechanism further comprises a balance wheel.
 4. The automatic injection device of claim 1, wherein the potential energy source is a spring configured to move the plunger.
 5. The automatic injection device of claim 4, wherein the spring is directly connected to the plunger.
 6. The automatic injection device of claim 1, wherein the wire and the at least one pulley are configured to convert rotational movement of the at least one set of gears into a linear motion.
 7. The automatic injection device of claim 1, wherein the regulator further comprises an electric circuit that measures time and controls release of the potential energy from the potential energy source over the proscribed period of time. 